Allele Registry

Canonical Allele Identifier: PA2499260214

Gene: FLG HGNC NCBI

ClinVar RCV:

RCV001671068

ClinVar Variation:

1258538

HGVS (amino-acid)	Matching Registered Transcripts
NP_002007.1:p.Ser3935Pro	CA1102783 NM_002016.2:c.11803T>C